BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ORTHOVISC INJ

    MDR report key: 8569383 · Received April 30, 2019

    Report

    Report Number
    MW5086306
    Event Type
    Injury
    Date Received
    April 30, 2019
    Date of Event
    April 24, 2019
    Report Date
    April 24, 2019
    Manufacturer
    ANIKA THERAPEUTICS INC.
    Product Code
    MOZ
    UDI-DI
    59676036001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    ORTHOVISC WAS PRESCRIBED FOR OSTEOARTHRITIS TO BE INJECTED INTO THE LEFT SHOULDER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    358706 ORTHOVISC INJ ACID, HYALURONIC INTRAVASCULAR MOZ ANIKA THERAPEUTICS INC. 59676036001

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR